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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964731copy number variation1nstd209human GRCh38 chr22: 39,063,170-39,075,354 , GRCh37.p13 chr22: 39,459,175-39,471,359 APOBEC3G, LOC107985563
    nsv5918566copy number variation1nstd209human GRCh38 chr9: 15,488,092-15,488,782 , GRCh37.p13 chr9: 15,488,090-15,488,780 PSIP1
    nsv5916583copy number variation1nstd209human GRCh38 chr9: 15,474,543-15,474,839 , GRCh37.p13 chr9: 15,474,541-15,474,837 PSIP1
    nsv5722589mobile element insertion2nstd211human GRCh38 chr7: 44,799,072-44,799,072 , GRCh37.p13 chr7: 44,838,671-44,838,671 PPIA
    nsv5629293insertion1nstd207human GRCh38 chr9: 15,488,804-15,488,804 , GRCh37.p13 chr9: 15,488,802-15,488,802 PSIP1
    nsv5556950sequence alteration1nstd206human GRCh38 chr7: 44,712,903-47,388,095 , GRCh37.p13 chr7: 44,752,502-47,427,692 , ADCY1, 51 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5553878insertion1nstd206human GRCh38 chr9: 15,477,500-15,477,530 , GRCh37.p13 chr9: 15,477,498-15,477,528 PSIP1
    nsv5536003copy number variation1nstd206human GRCh38 chr22: 39,082,189-39,082,255 , GRCh37.p13 chr22: 39,478,194-39,478,260 APOBEC3G
    nsv5491322copy number variation1nstd206human GRCh38 chr7: 44,802,945-44,803,203 , GRCh37.p13 chr7: 44,842,544-44,842,802 PPIA
    nsv5483195copy number variation1nstd206human GRCh38 chr9: 15,474,543-15,474,840 , GRCh37.p13 chr9: 15,474,541-15,474,838 PSIP1
    nsv5478904copy number variation1nstd206human GRCh38 chr9: 15,488,841-15,489,517 , GRCh37.p13 chr9: 15,488,839-15,489,515 PSIP1
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5364692translocation1nstd200human GRCh38 chr9: 15,474,543-15,474,543 , GRCh38 chr9: 15,474,840-15,474,840 , GRCh37.p13 chr9: 15,474,541-15,474,541 , GRCh37.p13 chr9: 15,474,838-15,474,838 PSIP1
    nsv5288097copy number variation1nstd204human GRCh38.p13 chr22: 38,982,101-39,534,900 , GRCh37.p13 chr22: 39,378,106-39,930,905 APOBEC3C, COX5BP7, 25 more genes
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5264980copy number variation1nstd204human GRCh38.p13 chr11: 65,876,001-66,092,800 , GRCh37.p13 chr11: 65,643,472-65,860,271 , LOC100420020, 17 more genes
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